Phase 1/2 Study of ETX-636 in Participants With Advanced Solid Tumors
Phase 1/2, open-label study of ETX-636 in participants with advanced solid tumors
Inclusion Criteria
- Metastatic or locally advanced and unresectable solid tumor that has progressed on or after at least one available therapy.
- Tumor harboring an activating PIK3CA mutation detected in either tumor tissue or ctDNA.
- At least 1 measurable lesion or evaluable disease per RECIST v1.1.
- An ECOG performance status score of 0 or 1.
- Adequate organ function. Additional key inclusion criterion for Parts B and C:
- Confirmed metastatic or locally advanced HR+/HER2- breast cancer not amenable to surgical resection with curative intent and must have received at least 1 prior CDK4/6 inhibitor and at least 1 prior anti-estrogen therapy. Key
Exclusion Criteria
- Has history (within ≤2 years before screening) of a solid tumor or hematological malignancy that is histologically distinct from the cancers being studied.
- Has symptomatic brain or spinal metastases or a known or suspected history of untreated or uncontrolled central nervous system (CNS) involvement.
- Has an established diagnosis of diabetes mellitus type 1 or has uncontrolled diabetes mellitus type 2.
- Has received treatment with any local or systemic anticancer therapy or investigational anticancer agent within 14 days prior to start of treatment.
- Has toxicities from previous anticancer therapies that have not resolved to baseline levels with the exception of alopecia and peripheral neuropathy.
- Has had radiotherapy outside the target tumor lesions within 14 days prior to start of treatment.
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT06993844.
Locations matching your search criteria
United States
California
San Francisco
Connecticut
New Haven
Massachusetts
Boston
Texas
Houston
Washington
Seattle
Brief Summary: This is a Phase 1/2, open-label, multicenter, 3-part study to evaluate the
safety, tolerability, PK, PD, and preliminary efficacy of ETX-636 in participants with
advanced solid tumors harboring a PIK3CA mutation.
Part A will evaluate escalating doses of ETX-636 as monotherapy in participants with
advanced solid tumors. Part B will evaluate escalating doses of ETX-636 as combination
therapy with fixed dose fulvestrant in participants with hormone receptor positive (HR+),
HER2 negative (HER2-) locally advanced or metastatic breast cancer. Part C will be a
combination therapy expansion in participants with HR+, HER2- locally advanced or
metastatic breast cancer.
Each study part will include a 28-day screening period, followed by treatment with
ETX-636 monotherapy or combination therapy.
Trial PhasePhase I/II
Trial Typetreatment
Lead OrganizationEnsem Therapeutics
- Primary IDETX636-C-001
- Secondary IDsNCI-2025-05482
- ClinicalTrials.gov IDNCT06993844